Bis(tri-tert-butylphosphine)palladium(0) CAS 53199-31-8 Purity ≥98.0% Pd ≥20.2%

Short Description:

Name: Bis(tri-tert-butylphosphine)palladium(0)

Synonyms: Fu Catalyst; Pd(t-Bu3P)2

CAS: 53199-31-8

Purity: ≥98.0% (T)

Pd: ≥20.2%

Appearance: White Crystalline Powder

E-Mail: alvin@ruifuchem.com

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Product Detail

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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer of Bis(tri-tert-butylphosphine)palladium(0) (CAS: 53199-31-8) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name	Bis(tri-tert-butylphosphine)palladium(0)
Synonyms	Fu Catalyst; Pd(t-Bu3P)2
CAS Number	53199-31-8
CAT Number	RF-PI2205
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C24H54P2Pd
Molecular Weight	511.06
Melting Point	>300℃
Solubility	Soluble in Toluene Benzene, Slight Soluble in Chloroform and Acetone
Sensitive	Hygroscopic; Light, Air & Moisture Sensitive
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White Crystalline Powder
Palladium (Pd)	≥20.2%
Purity	≥98.0% (T)
Total Metallic Impurities	≤1500ppm
Single Metallic Impurity	≤100ppm
1H NMR Spectrum	Conforms to structure
X-Ray Diffraction	Conforms to structure
Test Standard	Enterprise Standard

Package & Storage:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture

Advantages:

FAQ:

Application:

Bis(tri-tert-butylphosphine)palladium(0) (CAS: 53199-31-8) is used in Coupling reactions, Heck couplings. It acts as a palladium catalyst for reductive carbonylation, is used in carbonylation, oligomerization and other reactions. Introduced as an easier to handle Pd/P(t-Bu)3-based catalyst for the Negishi cross-coupling of aryl/vinyl chlorides. A versatile catalyst for the cross-coupling of aryl and vinyl chlorides. Catalyst for the amination of aryl chlorides and bromides using aqueous hydroxide bases. Useful catalyst for the cross-coupling of heteroaromatic carboxylic acids. Pd-catalyzed Newnan-Kwart rearrangement of O-aryl thiocarbamates. Cross-coupling of silanolates and halides. Elimination/isomerization of enol triflates derived from β-ketoesters.